Targeting Triple-Negative Breast Cancer by the Phytopolyphenol Carnosol: ROS-Dependent Mechanisms.
Halima AlsamriYusra Al DhaheriRabah IratniPublished in: Antioxidants (Basel, Switzerland) (2023)
Triple-negative breast cancer (TNBC), which lacks the expression of the three hormone receptors (i.e., estrogen receptor, progesterone receptor, and human epidermal growth factor receptor), is characterized by a high proliferative index, high invasiveness, poor prognosis, early relapse, and a tendency to be present in advanced stages. These characteristics rank TNBC among the most aggressive and lethal forms of breast cancer. The lack of the three receptors renders conventional hormonal therapy ineffective against TNBC. Moreover, there are no clinically approved therapies that specifically target TNBC, and the currently used chemotherapeutic agents, such as cisplatin, taxanes, and other platinum compounds, have a limited clinical effect and develop chemoresistance over time. Phytochemicals have shown efficacy against several types of cancer, including TNBC, by targeting several pathways involved in cancer development and progression. In this review, we focus on one phytochemical carnosol, a natural polyphenolic terpenoid with strong anti-TNBC effects and its ROS-dependent molecular mechanisms of action. We discuss how carnosol targets key pathways and proteins regulating the cell cycle, growth, epigenetic regulators, invasion, and metastasis of TNBC. This review identifies carnosol as a potential novel targeting protein degradation molecule.
Keyphrases
- poor prognosis
- cell cycle
- estrogen receptor
- epidermal growth factor receptor
- long non coding rna
- papillary thyroid
- endothelial cells
- cell death
- tyrosine kinase
- gene expression
- cell proliferation
- dna damage
- squamous cell
- advanced non small cell lung cancer
- reactive oxygen species
- stem cells
- young adults
- binding protein
- type diabetes
- risk assessment
- oxidative stress
- free survival
- metabolic syndrome
- childhood cancer
- smoking cessation
- cell migration
- breast cancer risk